Phenotype #0000039464
| Individual ID |
00052887 |
| Associated disease |
LCA |
| Phenotype details |
Leber congenital amaurosis; macular degeneration, absence of normal pupil response, pigmentary changes over time, poor or loss in night vision, nystagmus, severe rod-cone dystrophy, night blindness |
| Diagnosis/Initial |
- |
| Inheritance |
Isolated (sporadic) |
| Diagnosis/Definite |
- |
| Age/Examination |
- |
| Age/Diagnosis |
- |
| Age/Onset |
- |
| Phenotype/Onset |
- |
| Protein |
- |
| Owner name |
Muhammad Ajmal |
| Database submission license |
No license selected |
| Created by |
Muhammad Ajmal |
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